Variant report

Variant	esv1796367
Chromosome Location	chr7:97504247-97568276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:97544753-97545017	GM12878	blood:	n/a	n/a
2	BATF	chr7:97545127-97545322	GM12878	blood:	n/a	n/a
3	BATF	chr7:97532399-97532863	GM12878	blood:	n/a	n/a
4	BATF	chr7:97517798-97518101	GM12878	blood:	n/a	n/a
5	BATF	chr7:97517863-97518077	GM12878	blood:	n/a	n/a
6	BATF	chr7:97544706-97545031	GM12878	blood:	n/a	n/a
7	BATF	chr7:97541709-97541900	GM12878	blood:	n/a	n/a
8	BATF	chr7:97508909-97509359	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:97538914-97539187	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:97545138-97545312	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:97508956-97509366	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:97544694-97544995	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:97537513-97537758	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:97509132-97509377	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:97544643-97545002	GM12878	blood:	n/a	n/a
16	CBX3	chr7:97508845-97509104	K562	blood:	n/a	n/a
17	CBX3	chr7:97508766-97509173	K562	blood:	n/a	n/a
18	CEBPB	chr7:97545613-97545876	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:97557830-97557832	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:97559008-97559085	HepG2	liver:	n/a	chr7:97559036-97559047 chr7:97559038-97559047 chr7:97559036-97559049
21	CHD1	chr7:97557647-97557768	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:97541680-97541830	RPTEC	kidney:	n/a	n/a
23	CTCF	chr7:97541571-97542009	A549	lung:	n/a	n/a
24	CTCF	chr7:97557720-97557870	HCPEpiC	choroid plexus:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
25	CTCF	chr7:97521100-97521250	HEK293	kidney:	n/a	n/a
26	CTCF	chr7:97557720-97557870	SAEC	small airway:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
27	CTCF	chr7:97557720-97557870	GM12866	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
28	CTCF	chr7:97557563-97557990	K562	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
29	CTCF	chr7:97557700-97557850	GM06990	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
30	CTCF	chr7:97557638-97557943	GM12892	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
31	CTCF	chr7:97557700-97557850	HRE	kidney:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
32	CTCF	chr7:97557615-97557882	SK-N-SH_RA	brain:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
33	CTCF	chr7:97521120-97521270	GM12873	blood:	n/a	n/a
34	CTCF	chr7:97521239-97521246	A549	lung:	n/a	n/a
35	CTCF	chr7:97521100-97521250	GM12873	blood:	n/a	n/a
36	CTCF	chr7:97541640-97541790	A549	lung:	n/a	n/a
37	CTCF	chr7:97541799-97541903	Medullo	brain:	n/a	n/a
38	CTCF	chr7:97557656-97557940	H1-hESC	embryonic stem cell:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
39	CTCF	chr7:97557644-97557955	LNCaP	prostate:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
40	CTCF	chr7:97557712-97557887	MCF-7	breast:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
41	CTCF	chr7:97521100-97521250	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr7:97521100-97521250	HepG2	liver:	n/a	n/a
43	CTCF	chr7:97557700-97557850	GM12869	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
44	CTCF	chr7:97557720-97557870	HEK293	kidney:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
45	CTCF	chr7:97541696-97542028	K562	blood:	n/a	n/a
46	CTCF	chr7:97541640-97541790	HMF	breast:	n/a	n/a
47	CTCF	chr7:97557700-97557850	RPTEC	kidney:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
48	CTCF	chr7:97557700-97557850	HL-60	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
49	CTCF	chr7:97557720-97557870	AG09309	skin:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
50	CTCF	chr7:97557564-97557963	A549	lung:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97557827-97557877	Caco-2	colon:	n/a
2	chr7:97557827-97557877	Caco-2	colon:	n/a
3	chr7:97558753-97558803	AoSMC	blood vessel:	n/a
4	chr7:97557134-97557184	SK-N-MC	brain:	n/a
5	chr7:97557298-97557348	H1-hESC	embryonic stem cell:	embryo
6	chr7:97565504-97565554	BJ	skin:	n/a
7	chr7:97567812-97567862	ProgFib	skin:	n/a
8	chr7:97505608-97505658	K562	blood:	n/a
9	chr7:97557298-97557348	HCF	heart:	n/a
10	chr7:97565504-97565554	U87	brain:	n/a
11	chr7:97565504-97565554	SKMC	muscle:	n/a
12	chr7:97557827-97557877	GM12878	blood:	n/a
13	chr7:97557830-97557880	ECC-1	luminal epithelium:	n/a
14	chr7:97557298-97557348	A549	lung:	n/a
15	chr7:97557827-97557877	H1-hESC	embryonic stem cell:	embryo
16	chr7:97565354-97565404	NB4	blood:	n/a
17	chr7:97557134-97557184	NB4	blood:	n/a
18	chr7:97557298-97557348	LNCaP	prostate:	n/a
19	chr7:97565504-97565554	HCPEpiC	choroid plexus:	n/a
20	chr7:97557298-97557348	PrEC	prostate:	n/a
21	chr7:97557830-97557880	H1-hESC	embryonic stem cell:	embryo
22	chr7:97565504-97565554	ProgFib	skin:	n/a
23	chr7:97558753-97558803	MCF10A-Er-Src	breast:	n/a
24	chr7:97505608-97505658	PrEC	prostate:	n/a
25	chr7:97558075-97558125	CMK	blood:	n/a
26	chr7:97557830-97557880	CMK	blood:	n/a
27	chr7:97567812-97567862	MCF-7	breast:	n/a
28	chr7:97557830-97557880	HNPCEpiC	eye:	n/a
29	chr7:97557298-97557348	AoSMC	blood vessel:	n/a
30	chr7:97565504-97565554	SK-N-SH	brain:	n/a
31	chr7:97557830-97557880	RPTEC	kidney:	n/a
32	chr7:97557827-97557877	NHBE	bronchial:	n/a
33	chr7:97565504-97565554	GM19239	blood:	n/a
34	chr7:97557827-97557877	AG09319	gingival:	n/a
35	chr7:97567812-97567862	HCM	heart:	n/a
36	chr7:97568024-97568074	NHBE	bronchial:	n/a
37	chr7:97553776-97553826	HAEpiC	amniotic membrane:	n/a
38	chr7:97557298-97557348	HEEpiC	esophagus:	n/a
39	chr7:97553776-97553826	AG09309	skin:	n/a
40	chr7:97505608-97505658	A549	lung:	n/a
41	chr7:97567812-97567862	CMK	blood:	n/a
42	chr7:97565504-97565554	HepG2	liver:	n/a
43	chr7:97558075-97558125	SK-N-SH_RA	brain:	n/a
44	chr7:97557298-97557348	HIPEpiC	eye:	n/a
45	chr7:97565504-97565554	IMR90	lung:	fetal
46	chr7:97557298-97557348	GM19239	blood:	n/a
47	chr7:97553776-97553826	CMK	blood:	n/a
48	chr7:97557134-97557184	AG09309	skin:	n/a
49	chr7:97557134-97557184	HCPEpiC	choroid plexus:	n/a
50	chr7:97557827-97557877	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:97464795..97465461-chr7:97557301..97558244,2	K562	blood:
2	chr7:96733769..96734552-chr7:97557710..97558244,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAC1-1	chr7:97512594-97513107	NONHSAT122151
2	lnc-TAC1-2	chr7:97515180-97515386	NONHSAT122152
3	lnc-TAC1-3	chr7:97535741-97536134	NONHSAT122154

Variant related genes	Relation type
ENSG00000232097	TF binding region
ENSG00000231812	TF binding region
ENSG00000221048	TF binding region
ENSG00000232032	TF binding region
ENSG00000235982	TF binding region
RPS3AP29	TF binding region
ASNS	TF binding region
ENSG00000231859	TF binding region
ENSG00000232097	CpG island
ENSG00000231812	CpG island
ENSG00000221048	CpG island
ENSG00000232032	CpG island
ENSG00000235982	CpG island
RPS3AP29	CpG island
ASNS	CpG island
ENSG00000231859	CpG island

Extended variants
information (count: 1937 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1937 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6961291	chr7:97504281-97504282	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs2970204	chr7:97504283-97504284	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs3998623	chr7:97504294-97504295	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs554304071	chr7:97504335-97504336	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs6979298	chr7:97504336-97504337	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs3998624	chr7:97504364-97504365	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs35767990	chr7:97504388-97504389	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs6979333	chr7:97504391-97504392	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs543564537	chr7:97504395-97504396	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200483878	chr7:97504417-97504418	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs3998625	chr7:97504424-97504425	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs565039256	chr7:97504439-97504440	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs3957025	chr7:97504447-97504448	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs3998607	chr7:97504448-97504449	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs113642031	chr7:97504450-97504451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs3058485	chr7:97504473-97504474	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs532355328	chr7:97504532-97504533	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs199512827	chr7:97504552-97504553	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs200577728	chr7:97504571-97504572	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs541280369	chr7:97504594-97504595	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs3998608	chr7:97504599-97504600	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs144382516	chr7:97504600-97504601	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs559593229	chr7:97504650-97504651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs28635859	chr7:97504658-97504659	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs3998609	chr7:97504661-97504662	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs3957026	chr7:97504663-97504664	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs191200541	chr7:97504688-97504689	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs141102210	chr7:97504697-97504698	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs3998611	chr7:97504698-97504699	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs3957027	chr7:97504716-97504717	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs569976223	chr7:97504718-97504719	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs3957028	chr7:97504721-97504722	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs3957029	chr7:97504723-97504724	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs3998612	chr7:97504730-97504731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs6945593	chr7:97504774-97504775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs56849186	chr7:97504806-97504807	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs534281002	chr7:97504854-97504855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs6945774	chr7:97504895-97504896	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs552265940	chr7:97504896-97504897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs570668187	chr7:97504925-97504926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs186475823	chr7:97505518-97505519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs563663007	chr7:97505520-97505521	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs530820999	chr7:97505537-97505538	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs201239924	chr7:97505569-97505570	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs59320219	chr7:97505572-97505573	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs79395247	chr7:97505591-97505592	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs575118843	chr7:97505604-97505605	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs537040932	chr7:97505955-97505956	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs112122941	chr7:97505971-97505972	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs558624383	chr7:97505976-97505977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97502200-97504400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:97508800-97509000	Enhancers	Esophagus	oesophagus
3	chr7:97509000-97510400	Weak transcription	Esophagus	oesophagus
4	chr7:97518200-97518400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:97518200-97518400	Enhancers	Gastric	stomach
6	chr7:97527600-97557200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr7:97536800-97557200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr7:97540000-97557600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:97541400-97542200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:97541400-97542200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:97542200-97545600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr7:97542200-97546000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr7:97542200-97574200	Weak transcription	Primary B cells from peripheral blood	blood
14	chr7:97542800-97546400	Weak transcription	Brain Angular Gyrus	brain
15	chr7:97544400-97545800	Enhancers	GM12878-XiMat	blood
16	chr7:97544600-97549800	Weak transcription	Pancreas	Pancrea
17	chr7:97544800-97547400	Weak transcription	Aorta	Aorta
18	chr7:97545600-97546400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr7:97545800-97546200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:97545800-97546400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr7:97545800-97546400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr7:97545800-97546400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr7:97545800-97546400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr7:97545800-97546400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr7:97546000-97546400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:97546000-97546400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr7:97546000-97546400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr7:97546000-97546400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:97546000-97546400	Enhancers	Fetal Brain Male	brain
30	chr7:97546000-97546800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:97546400-97556800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:97546400-97557000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:97548800-97549800	Enhancers	Colonic Mucosa	Colon
34	chr7:97548800-97549800	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr7:97548800-97549800	Enhancers	Stomach Mucosa	stomach
36	chr7:97554600-97557400	Weak transcription	Esophagus	oesophagus
37	chr7:97555800-97556000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr7:97556000-97557000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr7:97556600-97557600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
40	chr7:97556600-97557800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
41	chr7:97556600-97557800	Active TSS	Brain Angular Gyrus	brain
42	chr7:97556800-97557000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
43	chr7:97556800-97557000	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr7:97556800-97557800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
45	chr7:97556800-97557800	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:97556800-97557800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
47	chr7:97556800-97557800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr7:97556800-97557800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr7:97556800-97557800	Active TSS	Brain Cingulate Gyrus	brain
50	chr7:97556800-97557800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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